Orthovita, Inc.
Orthovita, Inc. holds FDA 510(k) medical device clearances, first cleared 2001, most recent 2017.
Top product codes for Orthovita, Inc.
Recent clearances by Orthovita, Inc.
- K163621 — Vitoss Bioactive (BA) Injectable
- K161447 — HydroSet XT
- K153608 — Vitoss BiModal Bone Graft Substitute Foam Strip
- K153306 — Imbibe Needle
- K140868 — STRYKER KWIC NEEDLE
- K140414 — IMBIBE NEEDLE
- K103173 — VITOSS BA BIMODAL BIOACTIVE BONE GRAFT SUBSTITUTE
- K101171 — ORTHOVITA PEEK SPACER
- K102545 — FM-02 BONE GRAFT SUBSTITUTE
- K091618 — VITOMATRIX
- K080108 — CORTOSS BONE AUGMENTATION MATERIAL
- K083033 — VITOSS BONE GRAFT SUBSTITUTE, BONE GRAFT SUBSTITUTE FILLED CANISTER, FOAM & BIOACTIVE FOAM BONE GRAFT SUBSTITUTE
- K081439 — VITOSS BIOACTIVE FOAM PACK BONE GRAFT SUBSTITUTE
- K072184 — VITOSS BIOACTIVE FOAM BONE GRAFT SUBSTITUTE
- K052173 — VITAGEL SURGICAL HEMOSTAT SPRAY SET
- K050795 — IMBIBE BONE MARROW ASPIRATION NEEDLE
- K032288 — VITOSS SCAFFOLD FOAM BONE GRAFT MATERIAL
- K032812 — ENDOSKELETON TA VERTEBRAL BODY REPLACEMENT
- K032130 — VITOSS-FILLED CARTRIDGE
- K032409 — VITOSS SCAFFOLD SYNTHETIC CANCELLOUS BONE VOID FILLER
- K030208 — IMBIBE II SYRINGE
- K023074 — IMBIBE BONE MARROW ASPIRATION SYRINGE
- K011087 — ORTHOVITA PISTON SYRINGE OR IMBIBE BONE MARROW ASPIRATION SYRINGE
Data sourced from openFDA. This site is unofficial and independent of the FDA.